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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19861생성일: 2026년 10월 25일

3,4-Dichlorobenzeneboronic acid → (1-(3,4-dichlorophenyl)-5-(1-isopropylpiperidin-4-yloxy)-1H-indol-2-yl)(4,4-difluoropiperidin-1-yl)methanone

https://huagongshe.com/reaction/19861

반응식

참여 물질

역할이름HCID투입량
반응물3,4-Dichlorobenzeneboronic acidHCID 2734330—
반응물(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
생성물(1-(3,4-dichlorophenyl)-5-(1-isopropylpiperidin-4-yloxy)-1H-indol-2-yl)(4,4-difluoropiperidin-1-yl)methanoneHCID 16739525—

반응 단계

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 3,4-dichlorophenylboronic acid. The title compound was obtained in 81% yield as yellow foam. MS (m/e): 550.2 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d4bb8722977941e6945f970d1a5873ce
출처 메모uspto-grants-2010_06